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商陆抗病毒蛋白基因在麝香百合中的转化和表达
引用本文:王进忠,王彦珺,王锡锋,张民照,高遐虹,孙淑玲,周广和.商陆抗病毒蛋白基因在麝香百合中的转化和表达[J].华北农学报,2005,20(6):77-79.
作者姓名:王进忠  王彦珺  王锡锋  张民照  高遐虹  孙淑玲  周广和
作者单位:北京农学院,植物科学技术系,北京,102206;北京市农业应用新技术重点实验室,北京,102206;北京农学院,植物科学技术系,北京,102206;中国农业科学院植物保护研究所,北京,100094
基金项目:北京市自然科学基金(5042018;5043026)
摘    要:以麝香百合叶片愈伤组织为受体,利用根瘤农杆菌介导法将美洲商陆蛋白(PAP)基因和抗卡那霉素筛选基因以共转化的方式转入百合叶片愈伤组织中,然后在含有MS培养基中筛选愈伤组织并得到再生植株,在建立的农杆菌转化百合的遗传转化体系中,获得49株再生植株,经PCR检测表明PAP基因已经转移到有抗性愈伤组织再生出百合植株中。

关 键 词:PAP基因  麝香百合  转化  表达
文章编号:1000-7091(2005)06-0077-03
收稿时间:2005-08-24
修稿时间:2005-08-24

Expression of Pokeweed Antiviral Protein Gene in the Callus of Lilium longiflorum by Agrobacterium-mediated Transformation
WANG Jin-zhong,WANG Yan-jun,WANG Xi-feng,ZHANG Min-zhao,GAO Xia-hong,SUN Shu-ling,ZHOU Guang-he.Expression of Pokeweed Antiviral Protein Gene in the Callus of Lilium longiflorum by Agrobacterium-mediated Transformation[J].Acta Agriculturae Boreali-Sinica,2005,20(6):77-79.
Authors:WANG Jin-zhong  WANG Yan-jun  WANG Xi-feng  ZHANG Min-zhao  GAO Xia-hong  SUN Shu-ling  ZHOU Guang-he
Institution:1 .Department of Plant Science and Technology,Beijing Agricultural College,Beijing 102206,China; 2. Beijing Key Laboratory of New Technology in Agricultural Application, Beijing 102206, China; 3. Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100094, China
Abstract:We report an efficient transformation protocol for stable introduction of PAP gene into callus of lily leaf. Calli of Liliura longiflorura leaf were inoculated with Agrobacteriura tumefaciens strain LBA4404 containing the binary vector PBI121 - 1 harboring pokeweed antiviral protein gene,which was isolated from pokeweed leaves. In the selection of antibiotics, the calli of lily were inoculated with Agrobacterium containing PBI121 - 1 produced small amount of callus on 75 mg/L kanamycin and 250 mg/L cefotasimine selection plates. Plants were regenerated from resistant calli gained from the slectable medium with MS. An optimum protocol of transformation has been established and 49 regenerative plants from transformations have been obtained. The PAP eDNA integrated into the calli of lily was assayed by PCR, The PCR analyses demonstrated stable integration of PAP gene into the Liliura longiflorura genomes. Expression of the genes was particularly eminent in leaf tissue of primary transformant plants. The establishment of an efficient transformation method may facilitate the improvement of lily in terms of the levels of antiviral protein.
Keywords:Pokeweed antiviral protein(PAP)  Lilium longiflorum  Transformation  Expression  
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